메뉴 건너뛰기




Volumn 25, Issue 1, 2010, Pages 29-37

Synthesis and leishmanicidal activity of 2,3,4-substituted-5-imidazolones

Author keywords

Imidazolone; Leishmania major; Leishmanicidal activity; Substitution effect

Indexed keywords

2 METHYL 3 PHENYL 5 [2 THIENYLMETHYLIDENE] 3,5 DIHYDRO 4H IMIDAZOL 4 ONE; 2 METHYL 3 PHENYL 5 [PHENYLMETHYLIDENE] 3,5 DIHYDIDRO 4H MIDAZOLE 4 ONE; 2,3 DIPHENYL 5 [PHENYLMETHYLIDENE] 3,5 DIHYDRO 4H IMIDAZOLE 4 ONE; 3 (2 METHOXYPHENYL) 2 METHYL 5 [2 THIENYLMETHYLIDENE] 3,5 DIHYDRO 4H IMIDAZOL 4 ONE; 3 (3 METHOXYPHENYL) 2 METHYL 5 [2 THIENYLMETHYLIDENE] 3,5 DIHYDRO 4H IMIDAZOL 4 ONE; 3 (3 METHOXYPHENYL) 2 PHENYL 5 [ 2 THIENYLMETHYLIDENE 3,5 DIHYDRO 4H IMIDAZOL 4 ONE; 3 (4 METHOXYPHENYL) 2 METHYL 5 [2 THIENYLMETHYLIDENE] 3,5 DIHYDRO 4H IMIDAZOL 4 ONE; 3 (4 METHOXYPHENYL) 2 PHENYL 5 [2 THIENYLMETHYLIDENE 3,5 DIHYDRO 4H IMIDAZOL 4 ONE; 3 (5 METHOXYPHENYL) 2 METHYL 5 [2 THIENYLMETHYLIDENE] 3,5 DIHYDRO 4H IMIDAZOL 4 ONE; 5 [(1,1' BIPHENYL) 4 YLMETHYLIDENE] 2,3 DIPHENYLIDENE 3,5 DIHYDRO 4H IMIDAZOLE 4 ONE; 5 [(1,1' BIPHENYL) 4 YLMETHYLIDENE] 3 (3 METHOXYPHENYL) 2 METHYL 3,5 DIHYDRO 4H IMIDAZOLE 4 ONE; 5 [(1,1' BIPHENYL)4 YLMETHYLIDENE] 3(3 METHOXYPHEYNYL) 2 PHENYL 3,5 DIHYDRO 4H IMIDAZOLE 4 ONE; 5 [(1,1' BIPHENYL)4 YLMETHYLIDENE] 3(4 METHOXYPHEYNYL) 2 PHENYL 3,5 DIHYDRO 4H IMIDAZOLE 4 ONE; 5 [(1,1' BIPHENYL] 4 YLMETHYLIDENE] 3 (2 METHOXYPHENYL 2 PHENYL 3,5 DIHYDRO 4H IMIDAZOLE 4 ONE; 5 [(1,1' DIPHENYL) 4 YLMETHYLIDENE] 2 METHYL 3 PHENYL 3,5 DIHYDRO 4H IMIDAZOLE 4 ONE; 5 [(2 CHLORO 5 NITROPHENYL)METHYLIDENE] 3 (4 METHOXYPHENYL)2 PHENYL 3,5 DIHYDRO 4H IMIDAZOLE 4 ONE; 5 [(4 FLUOROPHENYL)METHYLIDENE] 2 METHYL 3 PHENYL 3,5 DIHYDRO 4H IMIDAZOLE 4 ONE; 5 [(4 FLUOROPHENYL)METHYLIDENE] 3 (2 METHOXYPHENYL)2 METHYL 3,5 DIHYDRO 4H IMIDAZOLE 4 ONE; 5 [(4 FLUOROPHENYL)METHYLIDENE] 3 (3 METHOXYPHENYL)2 METHYL 3,5 DIHYDRO 4H IMIDAZOLE 4 ONE; AMPHOTERICIN B; IMIDAZOLE DERIVATIVE; PENTAMIDINE; UNCLASSIFIED DRUG;

EID: 74349124358     PISSN: 14756366     EISSN: 14756374     Source Type: Journal    
DOI: 10.3109/14756360902932768     Document Type: Article
Times cited : (15)

References (24)
  • 2
    • 0027249951 scopus 로고
    • Practical progress and new drugs for changing patterns of leishmaniasis
    • Olliaro PL, Bryceson ADM. Practical progress and new drugs for changing patterns of leishmaniasis. Parasitol Today 1993;9:323-328
    • (1993) Parasitol Today , vol.9 , pp. 323-328
    • Olliaro, P.L.1    Bryceson, A.D.M.2
  • 3
    • 0029829697 scopus 로고    scopus 로고
    • Progress in chemotherapy of leishmaniasis
    • Ram VJ, Nath M. Progress in chemotherapy of leishmaniasis. Curr Med Chem 1996;3:303-328
    • (1996) Curr Med Chem , vol.3 , pp. 303-328
    • Ram, V.J.1    Nath, M.2
  • 5
    • 3543140068 scopus 로고    scopus 로고
    • Targeting Leishmania (L.) chagasi amastigotes through macrophage scavenger receptors: The use of drugs entrapped in liposomes containing phosphatidylserine
    • Tempone AG, Perez D, Rath S, Vilarinho AL, Mortara RA, Andrade HF Jr. Targeting Leishmania (L.) chagasi amastigotes through macrophage scavenger receptors: the use of drugs entrapped in liposomes containing phosphatidylserine. J Antimicrob Chemother 2004;54:60-68
    • (2004) J Antimicrob Chemother , vol.54 , pp. 60-68
    • Tempone, A.G.1    Perez, D.2    Rath, S.3    Vilarinho, A.L.4    Mortara, R.A.5    Andrade Jr., H.F.6
  • 6
    • 0035540414 scopus 로고    scopus 로고
    • New novel synthesis and antibacterial activity of 1-(substituted phenyl)-2-phenyl- 4-(39-halo, 49-hydroxy 59-methoxy benzylidene)-imidazole-5-one
    • Siddiqui SA, Bhusare SR, Jarikote DV, Pawar RP, Vibhute YB. New novel synthesis and antibacterial activity of 1-(substituted phenyl)-2-phenyl- 4-(39-halo, 49-hydroxy 59-methoxy benzylidene)-imidazole-5-one. Bull Korean Chem Soc 2001;22:1033-1036
    • (2001) Bull Korean Chem Soc , vol.22 , pp. 1033-1036
    • Siddiqui, S.A.1    Bhusare, S.R.2    Jarikote, D.V.3    Pawar, R.P.4    Vibhute, Y.B.5
  • 7
    • 0343145937 scopus 로고
    • The rearrangement and cyclization of Ethyl N- (methylaminoalkyl) carbanilates and 1,1-dimethyl-3-methylaminoalkyl- 3-phenylureas
    • Wright WB, Brabander JH. The rearrangement and cyclization of Ethyl N- (methylaminoalkyl) carbanilates and 1,1-dimethyl-3-methylaminoalkyl- 3-phenylureas. J Org Chem 1961;26:4051-4057
    • (1961) J Org Chem , vol.26 , pp. 4051-4057
    • Wright, W.B.1    Brabander, J.H.2
  • 8
    • 0000037844 scopus 로고
    • Imidazole derivatives for pharmaceutical preparations
    • Niedbalia V, Buettcher I. Imidazole derivatives for pharmaceutical preparations. Chem Abstr 1981;94:15732.
    • (1981) Chem Abstr , vol.94 , pp. 15732
    • Niedbalia, V.1    Buettcher, I.2
  • 9
    • 0023150712 scopus 로고
    • Some newer imidazolones and their anti-inflammatory activity
    • Pande K, Kalsi KR, Bhalla TN, Barthwal JP. Some newer imidazolones and their anti-inflammatory activity. Pharmazie 1987; 42:269.
    • (1987) Pharmazie , vol.42 , pp. 269
    • Pande, K.1    Kalsi, K.R.2    Bhalla, T.N.3    Barthwal, J.P.4
  • 10
    • 0013971089 scopus 로고
    • Central nervous system depressants I. 1-Aminoalkyl-3-aryl derivatives of 2-imidazolidinone, 2-imidazolidinethione, and tetrahydro-2(1H)- pyrimidinone
    • Wright WB, Brabander HS, Hardy RA, Osterberg AC. Central nervous system depressants I. 1-Aminoalkyl-3-aryl derivatives of 2-imidazolidinone, 2-imidazolidinethione, and tetrahydro-2(1H)- pyrimidinone. J Med Chem 1966;9:852-856
    • (1966) J Med Chem , vol.9 , pp. 852-856
    • Wright, W.B.1    Brabander, H.S.2    Hardy, R.A.3    Osterberg, A.C.4
  • 11
    • 0014446497 scopus 로고
    • Derivatives of imidazole. III. Synthesis and pharmacological activities of nitriles, amides, and carboxylic acid derivatives of imidazo[1,2-a]pyridine
    • Lingi A, Alfonso M, Pierluigi R, Afro G, Enzo Z, Nicola DT, et al. Derivatives of imidazole. III. Synthesis and pharmacological activities of nitriles, amides, and carboxylic acid derivatives of imidazo[1,2-a]pyridine. J Med Chem 1969;12:122-126
    • (1969) J Med Chem , vol.12 , pp. 122-126
    • Lingi, A.1    Alfonso, M.2    Pierluigi, R.3    Afro, G.4    Enzo, Z.5    Nicola, D.T.6
  • 12
    • 0015309896 scopus 로고
    • DL-1-(α-Methylbenzyl)-2-methylimidazole- 5-carboxylate esters. Synthesis and pharmacological properties
    • Brik F, Godefrot, Reatge J. DL-1-(α-Methylbenzyl)-2- methylimidazole- 5-carboxylate esters. Synthesis and pharmacological properties. J Med Chem 1972;15:336-337
    • (1972) J Med Chem , vol.15 , pp. 336-337
    • Brik, F.1    Godefrot, R.J.2
  • 13
    • 0016176190 scopus 로고
    • Monoamine oxidase inhibitory and anticonvulsant properties of 1,2, 4-trisubstituted 5-imidazolones
    • Verma M, Charturvedi AK, Chaudhary A, Parmar SS. Monoamine oxidase inhibitory and anticonvulsant properties of 1, 2, 4-trisubstituted 5-imidazolones. J Pharm Sci 1974;463:1740-1744
    • (1974) J Pharm Sci , vol.463 , pp. 1740-1744
    • Verma, M.1    Charturvedi, A.K.2    Chaudhary, A.3    Parmar, S.S.4
  • 14
    • 0026317555 scopus 로고
    • Possible anticonvulsant imidazloinones. Synthesis and anticonvulsant activity of 1N-(?9-picolinyl)-4-subsitutedbenzylidene- 2-methyl/phenyl-5- imidazolinone
    • Upadhyay P, Pandya A, Parekh H. Possible anticonvulsant imidazloinones. Synthesis and anticonvulsant activity of 1N-(?9-picolinyl)-4- subsitutedbenzylidene- 2-methyl/phenyl-5-imidazolinone. J Indian Chem Soc 1991;68:296-298
    • (1991) J Indian Chem Soc , vol.68 , pp. 296-298
    • Upadhyay, P.1    Pandya, A.2    Parekh, H.3
  • 17
    • 68049108342 scopus 로고    scopus 로고
    • In vitro antileishmanial activities of germatarnyl and silicon incorporated diorganotin derivatives: Synthesis and spectroscopic properties
    • Salma U, Mazhar M, Imtiaz-ud-Din, Ali S, Khan KM. In vitro antileishmanial activities of germatarnyl and silicon incorporated diorganotin derivatives: synthesis and spectroscopic properties. J Enzyme Inhib Med Chem 2009;23:413-419
    • (2009) J Enzyme Inhib Med Chem , vol.23 , pp. 413-419
    • Salma, U.1    Mazhar, M.2    Imtiaz-Ud-Din Ali, S.3    Khan, K.M.4
  • 19
    • 42949118439 scopus 로고    scopus 로고
    • In vitro leishmanicidal activity of 3-substituted isocoumarins: Synthesis and structure-activity relationship
    • Khan KM, Ahmed S, Khan ZA, Zia-Ullah, Rani M, Choudhary MI, et al. In vitro leishmanicidal activity of 3-substituted isocoumarins: synthesis and structure-activity relationship. Med Chem 2008;4:163-169
    • (2008) Med Chem , vol.4 , pp. 163-169
    • Khan, K.M.1    Ahmed, S.2    Khan, Z.A.3    Zia-Ullah Rani, M.4    Choudhary, M.I.5
  • 20
    • 0037375616 scopus 로고    scopus 로고
    • Synthesis and in vitro leishmanicidal activity of some hydrazides and their analogs
    • Khan KM, Rasheed M, Zia-Ullah, Hayat S, Kaukab F, Choudhary MI, et al. Synthesis and in vitro leishmanicidal activity of some hydrazides and their analogs. Bioorg Med Chem 2003;11:1381-1387
    • (2003) Bioorg Med Chem , vol.11 , pp. 1381-1387
    • Khan, K.M.1    Rasheed, M.2    Zia-Ullah Hayat, S.3    Kaukab, F.4    Choudhary, M.I.5
  • 21
    • 0000785501 scopus 로고
    • A ratio of 1:10 of oxazolone to PPA was used to get E-isomer; (B) Rao YS. A new stereospecific synthesis of the e isomers of 2-phenyl-4- arylmethylene-2-oxazolin-5-ones
    • (a) A ratio of 1:10 of oxazolone to PPA was used to get E-isomer; (b) Rao YS. A new stereospecific synthesis of the E isomers of 2-phenyl-4- arylmethylene-2-oxazolin-5-ones. J Org Chem 1976;41:722-725.
    • (1976) J Org Chem , vol.41 , pp. 722-725


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.